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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29532생성일: 2026년 10월 24일

Binap, (A+-)- → N-[4-Chloro-2(pyridine-4-carbonyl)-phenyl]-4-(1,1-dioxo-thiomorpholin-4-yl)-benzenesulfonamide

https://huagongshe.com/ko/reaction/29532

반응식

참여 물질

역할이름HCID투입량
반응물Binap, (A+-)-HCID 634876—
반응물Thiomorpholine 1,1-dioxideHCID 6484228—
반응물4-Bromo-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamideHCID 10072530—
반응물Potassium phosphate, tribasic, monohydrateHCID 22031701—
촉매PalladiumHCID 23938—
용매1,4-DioxaneHCID 31275—
생성물N-[4-Chloro-2(pyridine-4-carbonyl)-phenyl]-4-(1,1-dioxo-thiomorpholin-4-yl)-benzenesulfonamideHCID 59788575—

반응 단계

The title compound was prepared according to the general procedure for the synthesis of heterocyclyl and heteroaryl substituted phenylsulfonyl derivatives previously described, using 4-Bromo-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamide 0.3 g (0.66 mmol), potassium phosphate tribasic monohydrate 0.91 g (3.96 mmol), rac-2,2′-bis (diphenylphosphino)-1,1′-binaphthyl 0.12 g (0.198 mmol), thiomorpholine 1,1-dioxide 0.44 g (3.3 mmol) and Pd (dba)3 60 mg (0.066 mmol) in 6 ml dioxane, followed by work up and HPLC purification: LC-MSD, m/z for C22H20ClN3O3S2 [M+H]+: 502

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-bc22d2ac57ca47c6b71cce111ebcf138
출처 메모uspto-grants-2008_09